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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Wellbutrin SR (Bupropion). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (74)
Cases resulting in a serious event (64)
Cases resulting in death (6)
Cases resulting in life threatening events (3)
Cases resulting in hospitalization (15)
Cases resulting in disability (5)
Cases resulting in other serious reactions (46)
Below is a sample of reports where side effects / adverse reactions may be related to Wellbutrin SR (Bupropion). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 52 year old female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: 52 year old female
Adverse reactions / side effects: Dyspnoea Exertional, Chest Discomfort, Dyspnoea, Oedema Peripheral, Orthopnoea, Cardiac Failure Congestive
Adverse event resulted in: disablity
Suspect drug(s):
Wellbutrin SR (Bupropion)
Other drugs received by patient: Lunesta; Lexapro; Diovan; Aspirin; Prevacid; Benadryl
Adverse event in 18 year old female receiving Wellbutrin SR (Bupropion)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-17
Patient: 18 year old female
Adverse reactions / side effects: Generalised Anxiety Disorder, Overdose, Pyrexia, Hallucination, Convulsion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Wellbutrin SR
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Tylenol (Caplet)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Gravol TAB
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a physician from United States on 2007-10-16
Patient: female, weighing 68.5 kg (150.7 pounds)
Adverse reactions / side effects: Irritability
Suspect drug(s):
Wellbutrin SR (Bupropion)
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-10-15
Patient: female, weighing 65.8 kg (144.7 pounds)
Adverse reactions / side effects: Weight Decreased, Drug Ineffective, Therapeutic Response Unexpected With Drug Substitution, Bundle Branch Block, Gastric PH Decreased, Oesophageal Carcinoma, Pharmaceutical Product Complaint, Cardiac Disorder, Gastric Cancer
Suspect drug(s):
Wellbutrin SR (Bupropion)
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a physician from United States on 2007-10-12
Patient: female
Adverse reactions / side effects: Drug Effect Decreased, Drug Ineffective, Insomnia, Headache
Suspect drug(s):
Wellbutrin SR
Topamax
Adverse event in 58 year old female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-10-12
Patient: 58 year old female, weighing 83.9 kg (184.6 pounds)
Adverse reactions / side effects: Confusional State, Upper Limb Fracture, Pain, Joint Injury, Grand MAL Convulsion, Speech Disorder, Activities of Daily Living Impaired, Feeling Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Wellbutrin SR
Dosage: 100 or 150 once per day po
Administration route: Oral
Indication: Depression
Start date: 1997-12-01
End date: 2004-06-01
Wellbutrin XL
Dosage: 300 once per day po
Administration route: Oral
Indication: Depression
Start date: 2004-06-01
End date: 2007-09-01
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-10-03
Patient: female
Adverse reactions / side effects: Grand MAL Convulsion, Balance Disorder, Cognitive Disorder, Amnesia
Adverse event resulted in: hospitalization
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg twice per day
Administration route: Oral
Indication: Depression
Start date: 2002-01-01
End date: 2003-01-01
Wellbutrin XL
Dosage: 300mg per day
Administration route: Oral
Indication: Depression
Start date: 2003-01-01
End date: 2004-08-01
Other drugs received by patient: Concurrent Medications
Adverse event in 52 year old female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-10-01
Patient: 52 year old female
Adverse reactions / side effects: Chest Discomfort, Dyspnoea, Oedema Peripheral
Adverse event resulted in: disablity
Suspect drug(s):
Wellbutrin SR (Bupropion)
Other drugs received by patient: Lunesta; Lexapro; Diovan; Aspirin; Prevacid; Benadryl
Adverse event in 34 year old female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 34 year old female, weighing 101.4 kg (223.1 pounds)
Adverse reactions / side effects: Depression, Delivery, Deep Vein Thrombosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Paxil
Dosage: 20mg per day
Administration route: Oral
Start date: 1991-01-01
Wellbutrin SR
Dosage: 150mg per day
Administration route: Oral
Start date: 1991-01-01
Bupropion Hydrochloride
Administration route: Oral
Other drugs received by patient: Klonopin
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: female
Adverse reactions / side effects: Upper Limb Fracture, Fall
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg unknown
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Imitrex
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Bactroban
Administration route: Topical
Indication: Drug USE FOR Unknown Indication
Adverse event in 34 year old female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-27
Patient: 34 year old female, weighing 101.4 kg (223.1 pounds)
Adverse reactions / side effects: Depression, Delivery, Deep Vein Thrombosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Paxil
Dosage: 20mg per day
Administration route: Oral
Start date: 1991-01-01
Wellbutrin SR
Dosage: 150mg per day
Administration route: Oral
Start date: 1991-01-01
Bupropion Hydrochloride
Administration route: Oral
Other drugs received by patient: Klonopin
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-27
Patient: female
Adverse reactions / side effects: Upper Limb Fracture, Fall
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg unknown
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Imitrex
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Bactroban
Administration route: Topical
Indication: Drug USE FOR Unknown Indication
Adverse event in 21 year old female receiving Wellbutrin SR (Bupropion)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-25
Patient: 21 year old female, weighing 112.3 kg (247.1 pounds)
Adverse reactions / side effects: Grand MAL Convulsion, Contusion, Drug Effect Decreased, Drug Withdrawal Syndrome, Postictal State
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg twice per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-03-12
End date: 2007-04-27
Paxil
Dosage: 20mg twice per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Atenolol; Imitrex; Paxil; Elavil; Darvocet; Xanax
Adverse event in receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-23
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Foetal Arrhythmia
Suspect drug(s):
Wellbutrin SR (Bupropion)
Other drugs received by patient: Vitamin and Mineral Prenatal Supplement W / Folic Acid CAP
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-23
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Abortion Spontaneous
Suspect drug(s):
Wellbutrin SR (Bupropion)
Other drugs received by patient: Vitamin and Mineral Prenatal Supplement W / Folic Acid CAP
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-20
Patient: female
Adverse reactions / side effects: Ear Discomfort, Tinnitus, Dizziness Postural, Paraesthesia, Panic Attack, Joint Crepitation, Balance Disorder, Vertigo, Hearing Impaired, Vision Blurred, Disturbance in Attention, Memory Impairment, Depression, Deafness Transitory
Suspect drug(s):
Wellbutrin SR
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-06-04
Chantix
Indication: Smoking Cessation Therapy
Start date: 2007-06-11
Adverse event in 62 year old female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-07-20
Patient: 62 year old female, weighing 86.4 kg (190.1 pounds)
Adverse reactions / side effects: Barrett's Oesophagus
Suspect drug(s):
Wellbutrin XL
Dosage: 450mg per day
Administration route: Oral
Indication: Depression
Start date: 2003-10-01
Wellbutrin SR
Dosage: 150mg twice per day
Administration route: Oral
Indication: Depression
Start date: 1999-01-01
End date: 2003-10-01
Other drugs received by patient: Cymbalta; Effexor XR; Provigil
Adverse event in female receiving Wellbutrin SR (Bupropion)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-19
Patient: female, weighing 68.0 kg (149.7 pounds)
Adverse reactions / side effects: Therapeutic Response Unexpected With Drug Substitution, Condition Aggravated, Depression, Suicidal Ideation
Suspect drug(s):
Bupropion HCL
Dosage: 300 mg daily po
Administration route: Oral
Indication: Depression
Start date: 2007-05-01
End date: 2007-07-18
Wellbutrin SR
Adverse event in 32 year old male receiving Wellbutrin SR (Bupropion)
Reported by a pharmacist from United States on 2007-07-17
Patient: 32 year old male
Adverse reactions / side effects: Feeling Abnormal, Paraesthesia
Suspect drug(s):
Wellbutrin SR (Bupropion)
Adverse event in 30 year old female receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from Hungary on 2007-07-13
Patient: 30 year old female
Adverse reactions / side effects: Weight Decreased, Grand MAL Convulsion, Malaise, Mouth Haemorrhage, Insomnia, Circulatory Collapse
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg twice per day
Administration route: Oral
Indication: Depression
Start date: 2007-03-17
End date: 2007-06-10
Cymbalta
Dosage: 60mg twice per day
Administration route: Oral
Indication: Back Pain
Start date: 2007-03-17
End date: 2007-04-01
Xanax
Administration route: Oral
Indication: Insomnia
Start date: 2007-03-17
Adverse event in 45 year old female receiving Wellbutrin SR (Bupropion)
Reported by a pharmacist from Canada on 2007-07-10
Patient: 45 year old female
Adverse reactions / side effects: Overdose, Respiratory Arrest, Drug Dispensing Error, Convulsion, Loss of Consciousness
Suspect drug(s):
Wellbutrin XL
Dosage: 300mg per day
Indication: Drug USE FOR Unknown Indication
End date: 2006-07-03
Wellbutrin SR
Dosage: 100mg per day
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Lamictal
Adverse event in 29 year old male receiving Wellbutrin SR (Bupropion)
Reported by a consumer/non-health professional from United States on 2007-06-27
Patient: 29 year old male, weighing 88.6 kg (194.9 pounds)
Adverse reactions / side effects: Confusional State, Drug Ineffective, Amnesia, Fall, Loss of Consciousness, Paraesthesia, Tremor, Hyperventilation, Panic Attack, Syncope, Heart Rate Increased, Depressed Level of Consciousness, Depression, Epistaxis
Suspect drug(s):
Wellbutrin
Dosage: 450mg per day
Administration route: Oral
Indication: Major Depression
Wellbutrin SR
Dosage: 450mg per day
Administration route: Oral
Indication: Major Depression
Paxil
Dosage: 20mg at night
Administration route: Oral
Indication: Major Depression
Celexa
Dosage: 60mg at night
Indication: Major Depression
Start date: 2007-05-11
Other drugs received by patient: Inderal; Klonopin; Prozac; Zocor; Chlor-Trimeton; Multi-Vitamin; Bentyl; Prilosec
Adverse event in 41 year old male receiving Wellbutrin SR (Bupropion)
Reported by a lawyer from United States on 2007-06-21
Patient: 41 year old male
Adverse reactions / side effects: Fatigue, Completed Suicide, Disturbance in Attention, Depression, Asphyxia, Suicidal Ideation
Adverse event resulted in: death
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg twice per day
Administration route: Oral
Indication: Major Depression
Start date: 2005-05-04
End date: 2005-05-01
Paxil
Dosage: 10mg at night
Administration route: Oral
Indication: Major Depression
Start date: 2005-03-17
End date: 2005-03-01
Other drugs received by patient: Ambien; Celexa
Adverse event in 38 year old female receiving Wellbutrin SR (Bupropion)
Reported by a lawyer from United States on 2007-06-21
Patient: 38 year old female, weighing 52.7 kg (115.9 pounds)
Adverse reactions / side effects: Carbon Monoxide Poisoning, Completed Suicide
Adverse event resulted in: death
Suspect drug(s):
Wellbutrin SR (Bupropion)
Adverse event in male receiving Wellbutrin SR (Bupropion)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-19
Patient: male
Adverse reactions / side effects: Dyspnoea, Paranoia, Drug Ineffective, Restlessness, Physical Assault, Drug Withdrawal Syndrome, Amnesia, Irritability, Malaise, Hot Flush, Poisoning, Mood Swings, Altered State of Consciousness, Smoker
Suspect drug(s):
Paxil
Dosage: 20mg unknown
Administration route: Oral
Indication: Depression
Start date: 1999-01-01
Wellbutrin SR
Dosage: 150mg unknown
Administration route: Oral
Alcohol
Other drugs received by patient: Risperdal
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